System and method for the measurement of mechanical properties of elastic materials

ABSTRACT

A system and method for measuring the biomechanical properties of a healing wound in a specimen which utilize a chamber for applying an increasingly negative pressure over time to an area of tissue containing the wound, markings on the area for facilitating measurement of expansion of the area, a pressure measurement device for measuring the pressure in the chamber as a function of time, one or more cameras for obtaining multiple views of the area over time, a digitizer for generating a digital representation of each of the views, and a processor for determining a strain value from each digital representation and for correlating each strain value with a pressure measurement corresponding to the same point in time to provide a stress-strain relationship.

This is a continuation of co-pending application Ser. No. 08/064,334 nowU.S. Pat. No. 5,278,776 filed on May 19, 1993 which is a continuation ofSer. No. 07/703,398 filed on May 21, 1991, now abandoned.

FIELD OF THE INVENTION

The present invention relates generally to a method and apparatus formeasuring mechanical properties of a material; and, more specifically,to a method and apparatus for measuring certain biomechanical propertiesof a wound healing in tissue.

BACKGROUND OF THE INVENTION

The medical industry has desired to accurately measure the strength of ahealing to wound in tissue for a variety of reasons. With recent newinterest in cytokines, growth factors, and fetal regeneration,biomechanical studies of wound healing and tissue strength are becomingincreasingly more important.

The test specimens for such wound healing tests are laboratory animals,most typically rats. Conventionally, a cut or incision is made on theanimal, such as on the abdominal area, and the wound is permitted toheal for a certain time, typically a number of days. The pelt or skinarea around the wound is then carefully excised and the excised areamounted in a vise-like device. This device, called an Instrontensiometer, then stretches the pelt transversely to the wound directionand the breaking strength of the wound is measured. Unfortunately, thismethod introduces a number of factors tending to degrade the accuracyand usefulness of the test as the wound must be excised and measured invitro or outside of the body. For example, upon excision the pelt beginsdecomposition effecting its biomechanical properties and the excisingand handling of the pelt introduce stresses which may affect thestrength and sometimes even rupture relatively new wounds.

Another conventional in vitro method of wound strength testing isperformed using an air insufflated positive pressure device. However,this method also requires that the pelt be excised. In this method theexcised pelt is mounted between rings often with a thin elasticdiaphragm behind it and is subjected to positive pressure until thewound ruptures. Again, since the wound area is excised and manipulatedextensively, a great amount of error is introduced into the test.

While these methods have produced generally acceptable rupture strengthresults for wounds which have healed for several days, the errorintroduced is unacceptable on fragile and recent wounds and oftensignificantly obscures the results of tests on wounds imparted less thana few days before testing and on fragile fetal wounds. Compounding thedisadvantages of these in vitro methods is the fact that it is duringthe first few days after wounding when the wound is still quite fragilethat many of the drugs for which the effects are being tested exhibittheir most marked effect on wound healing. Further, since in vitro skincharacterization methods require excision of the wound, subcutaneousattachments and fibrin deposits which contribute to wound strength arenecessarily disrupted.

It would be desirable to test wounds with an increased accuracy andrepeatability, particularly with respect to relatively recent andotherwise fragile wounds such as fetal wounds. It would also bedesirable to measure biomechanical properties of skin in vivo, thus moreclosely measuring actual conditions when the skin is connected tosubcutaneous material. It would be further desirable to measurebiomechanical skin properties, such as elasticity, etc. withoutsubjecting the specimen to the trauma of excising, thus even permittinglimited biomechanical measurements, without rupture, on humans.

SUMMARY OF THE INVENTION

The present invention provides an apparatus for measuring in vivocertain mechanical and biomechanical properties of materials and tissuessuch as wounded skin. The apparatus is particularly effective fortesting the properties of fragile wounds, such as those imparted only afew days before testing and fetal tissue wounds.

In accordance with one aspect of the present invention, a device formeasuring the biomechanical properties of a healing wound in a specimenincludes a chamber for applying an increasingly negative pressure overtime to an area of tissue containing the wound, the area having markingsfor facilitating measurement of expansion of the area, a pressuremeasurement device for measuring the pressure in the chamber as afunction of time, a camera for obtaining multiple views of the area overtime, a digitizer for generating a digital representation of each of theviews, and a processor for determining a strain value from each digitalrepresentation and for correlating each strain value with a pressuremeasurement corresponding to the same point in time to provide astress-strain relationship.

In accordance with another aspect of the invention, a device formeasuring the mechanical properties of an elastic material includes achamber for applying an increasingly negative pressure over time to anarea of the material, the area including indicia facilitatingmeasurement of deformation of the area, a pressure measurementinstrument for measuring the pressure in the chamber as a function oftime, a camera for obtaining a number of views of the area over time, adigitizer for generating a digital representation of each of the views,and a processor for determining an expansion ratio from each digitalrepresentation and for correlating each expansion ratio with a pressuremeasurement corresponding to the same point in time.

In accordance with a further aspect of the invention, a method ofmeasuring the mechanical properties of an elastic material includes thesteps of marking the material with indicia facilitating tracking theexpansion of the material, applying an increasingly negative pressureover time to an area of the material including the indicia, measuringthe pressure applied to the area as a function of time, obtaining aplurality of views of the area over time, generating a digitalrepresentation of each of the views, and determining certain mechanicalcharacteristics of the material from the measured pressure and thegenerated digital representations.

These and other objects, advantages, features and aspects of the presentinvention will become apparent as the following description proceeds.

To the accomplishments of the foregoing and related ends, the invention,then comprises the features hereinafter fully described in thespecification and particularly pointed out in claims, the followingdescription and the annexed drawings setting forth in detail a certainillustrative embodiment of the invention, this being indicative,however, of but one of the various ways in which the principals of theinvention may be employed. It will be appreciated that the scope of theinvention is to be determined by the claims and the equivalents thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

In the annexed drawings:

FIG. 1 is a block diagram of a Vacuum Controlled Wound Chamber Devicefor in vivo testing of biomechanical skin properties in accordance withthe present invention;

FIG. 2 is a block diagram of the processing system of the VacuumControlled Wound Chamber Device;

FIG. 3 is an illustration of a wound on the abdominal region of alaboratory rat showing a ring and positional dot markings utilized inthe test;

FIGS. 4A and 4B represent a flowchart of the operation of the VacuumControlled Wound Chamber Device;

FIG. 5 is a graphical comparison of mean wound disruption strengths andstandard deviations for tests performed by the Vacuum Controlled WoundChamber Device over the first through fifth days following specimenwounding; and

FIG. 6 is a graphical comparison of wound disruption strengthsdetermined by the Vacuum Controlled Wound Chamber Device, the Instrontensiometer and an air insufflated positive pressure device.

DETAILED DESCRIPTION OF THE INVENTION

With reference to the several figures in which like reference numeralsdepict like items, and initially to FIG. 1, there is shown a blockdiagram of a Vacuum Controlled Wound Chamber Device (VCWCD) 10 formeasuring in vivo certain biomechanical properties of a healing wound.The VCWCD 10 includes a scale 12 upon which a specimen 14 having thewound is placed, a vacuum chamber 16 for the application of a negativepressure to the wound area, a vacuum controller 18, a vacuum source 20,one or more video cameras or charge coupled devices 22 having a view ofthe wound, a video recorder and image digitizer 24 and a processingsystem 26.

The specific embodiment of the VCWCD 10 illustrated and describedrelative to FIG. 1 is one designed to use a laboratory rat as the testspecimen having the healing wound which is tested. It will beappreciated, however, that the VCWCD 10 may be modified in a variety ofways to perform tests on other animal specimens or on non-biologicalmaterials, all of such modifications being within the scope of theinvention. Further, the operation of the VCWCD 10 will be describedbelow relative to a wound incised in the abdomen of the laboratory rat,it being apparent that the site of the wound is but a specific parameterof the test and that other wound sites may be chosen to evaluate thebiomechanical properties of healing wound tissue at other locations ofthe animal. Additionally, it is noted that the empirical data providedherein for the VCWCD 10, the Instron tensiometer, and the AirInsufflated Positive Pressure Device (AIPPD), was accumulated throughtests performed with the respective devices in accordance with theNational Research Council's guide for the care and use of laboratoryanimals.

The scale 12 is preferably an adjustable electronic scale which can betared to the weight of the test specimen, such as a Sartorius 1000MP9scale manufactured by Tennessee Scale Works. Positioned directly abovethe specimen 14 disposed on the scale 12 and in contact with a ring 30(shown greater detail in in FIG. 3) secured to the skin of the specimenis the vacuum chamber 16. The vacuum chamber 16 is of a generallycylindrical shape having an inner diameter for instance of 2.5 cm and isadapted to form a pressure seal with the ring 30. The vacuum chamber 16is preferably constructed of glass with at least the top portion of thevacuum chamber being transparent to allow a view of the wound to betaken by the video camera 22 which is positioned directly above thevacuum chamber. The vacuum chamber 16 also includes an orifice 32 forcommunication with the vacuum source 20. Both the vacuum chamber 16 andthe video camera 22 are vertically adjustable to accommodate theposition of the specimen and to permit the vacuum chamber and camera tobe lowered into a position where the chamber is in intimate contact withthe ring 30 while exerting minimal pressure on the ring and the woundarea.

The pressure in the vacuum chamber 16 is controlled by the vacuumcontroller 18 which adjusts the rate of communication with the vacuumsource 20. The vacuum controller 18 preferably includes a 248-10000 SVcontrol valve, a 250C controller, and a TORR type 122-AA-01000ABpressure transducer, all manufactured by MKS Instruments. The vacuumsource 20 is essentially a pump which maintains a very large volume at avery low pressure, the volume being large enough and the pressure beinglow enough to create a negative pressure in the vacuum chamber 16sufficient to rupture the wound. Consequently, when the vacuumcontroller 18 opens communication between the vacuum source 20 and thevacuum chamber 16, the air within the vacuum chamber will be evacuatedthrough the orifice 32 and suitable pressure lines, shown schematicallyas 36 and 38 in FIG. 1, to the vacuum source at a rate controlled by thevacuum controller.

The action of the vacuum controller 18 is controlled by the processingsystem 26 through a control signal shown schematically at 40. The vacuumcontroller 18 provides an analog electrical signal 42 proportional tothe negative pressure in the vacuum chamber 16 to the processing system26 which converts the analog signal to a digital equivalent and storesthe digital pressure data as a function of time.

The video camera 22 obtains a video image of the wound area of thespecimen through the vacuum chamber 16 and transmits that video image tothe video recorder and image digitizer 24 over the line 44. In otherembodiments of the invention it may be desireable to employ more thanone video camera to obtain different views of the wound area. The videorecorder and image digitizer 24 is preferably a Panasonic AG6300/60Hertz video recorder/playback unit and a Motion Analysis CorporationVP-110 Dynamic Image Processor equipped with a suitable interface to theprocessing system 26. Upon receiving an appropriate command from theprocessing system 26 over the line 46 in the form of an audio signal,the video recorder and image digitizer 24 (hereinafter, image digitizer)will begin to record the video signal from the video camera 22 onsuitable VHS recording media and to digitize the video signal at aspecific rate, such as two frames of digitized image data per second.These frames, which are digitized images of the wound area, arecollected and stored until the end of the test. Typically, 150 frames ofdigital images will adequately represent the test from the time when theinitial vacuum is applied to the wound until the wound disrupts. Onceall data has been collected for a test, the image digitizer 24 willtransfer the digital image frames to the processing system 26 over theline 48.

Upon completion of a test, the processing system 26 will have obtainedthe pressure data as a function of time from the vacuum controller 18 aswell as the digital images of the wound during the test as a function oftime from the image digitizer 24. The processing system 26 thus hassufficient data to allow the calculation of certain biomechanicalproperties, such as stress-strain relationships and modulus ofelasticity, for the wound being tested. The processing system 26 alsoprovides sufficient storage to allow the accumulation of data fromseveral tests, thus facilitating the statistical comparison of a seriesof tests having similar testing parameters, such as wound healing time.

The processing system 26 is shown in greater detail in FIG. 2. In thefigure dashed lines indicate the transfer of data while solid linesindicate control paths. The processing system 26 includes a testprocessor 50 which performs overall test control and calculates thefinal biomechanical properties of the test specimen, an image processor52 which processes the digitized image data, and display monitors 54, 56and keyboards 58, 60 corresponding to the test processor and the imageprocessor, respectively. The image processor 52 is preferably an IBM™compatible microcomputer based on an Intel™ 80386™ microprocessor chip.The image processor 52 preferably includes a dedicated video processingboard facilitating the processing of digital image data, such as a videoprocessing board manufactured by Motion Analysis Corporation which isconfigured for insertion into available slots in IBM™ compatiblemicrocomputers. During operation, the image processor 52 receivesdigital image frames of the wound area, indicated at 48, collectedduring a test from the image digitizer 24, processes those frames todetermine the location of specific dot indicators (which are applied tothe skin as described hereinafter) in the image and correlates thecoordinates of the dot indicators with the time from the beginning ofthe test. The keyboard 60 and display monitor 56 associated with thevideo processor 52 allow user interaction with the image processor 52,thereby allowing the user to input specific data to the image processorand permitting the user to edit digital displacement data to eliminateextraneous data, such as that data collected before a vacuum was appliedin the vacuum chamber and data collected after the wound was disrupted.The correlated, edited data 62 is then made available for transfer tothe test processor 50.

The test processor 50 is preferably also an IBM™ compatiblemicrocomputer employing an Intel™ 80386™ based microprocessor chip. Thetest processor 50 controls the vacuum controller 18 as well as the imagedigitizer 24. The test processor 50 further receives pressure data 42from the vacuum controller 18 which it digitizes and coordinates withtime from the beginning of a test. The test processor 50 coordinates thepressure data and digital displacement data of the indicator dots andperforms calculations of the biomechanical properties of the wound beingtested. The keyboard 58 and display monitor 54 associated with the testprocessor 50 provide user interaction with the test processor and allowthe user to edit the digitized pressure data to permit removal ofextraneous data, such as that gathered before a pressure was applied tothe wound and that collected after the wound disrupted.

To prepare a specimen rat for the test, the rat is administeredphenobarbital anesthesia intraperitoneally. An area of the rat, such asthe abdomen, is then shaved and cleaned. Using a template, a guide isdrawn for a midline abdominal incision of 2.5 cm, for example, and afull thickness incision is made following the guide. The wound is thenclosed, such as with surgical staples, and the animal is returned to itscage. The animal is fed ab libitum until the strength of the healingwound is tested.

When it is desired to test the strength of the wound, the rat isanesthetized and the circular ring 30 having an inner diametersubstantially corresponding to the length of the wound incision, forexample 2.5 cm, is secured, such as by gluing with cyanocrylate and/orusing surgical staples. Any surgical staples used previously to closethe incision are then removed. The effect of the circular ring 30 is toisolate the skin subject to the vacuum to a circular or truncatedspherical area of the skin, thus removing the contributions to thestress on the wound by the surrounding skin areas and providing auniform surface for an airtight seal with the vacuum chamber 16.

FIG. 3 illustrates a view of a ring 30 glued to the abdominal tissue 63of a laboratory rat 14 and positioned with the wound 64 bisecting thearea enclosed by the ring into equal halves. A pair of indicator dots 66are then inked onto the skin of the rat; one on each side of the wound64 as shown in FIG. 3, such that a line extending between the dots wouldintersect the approximate midpoint of the wound 64 perpendicular to thelongitudinal extent of the wound. While the embodiment of the testdescribed herein employs a par of indicator dots 66 to facilitatetracking expansion of the tissue during testing, any number of locatingindicia may be employed. Further, the wound area may be marked with amatrix of lines forming discrete areas facilitating calculations ofstresses, etc., at multiple locations over the wound area such as byfinite element methods or by other known methods.

The rat 14 is then placed abdomen up on the scale 12 and the scale istared. The vacuum chamber 16 and video camera 22 are then lowered untilthe lower surface of the vacuum chamber is in intimate contact with thering 30. The scale 12 is checked to ensure that the vacuum chamber 16does not exert a force upon the rat 14, as such a force may introduceerror into the test results.

The flowchart of FIGS. 4A mid 4B schematically illustrates the operationof the VCWCD 10 during a wound strength test. Note that reference tospecific steps in the flowchart of FIGS. 4A and 4B will be denoted inthe discussion below by a like reference numeral enclosed inparentheses, that solid lines in the figure represent the functionaltransfer between specific steps in the flowchart, and that dashed linesdenote the flow of data only. The circled "A" at the bottom of theflowchart in FIG. 4A indicates functional transfer to the same symbol atthe top of FIG. 4B.

Upon a command to the test processor 50 by an operator, such as througha sequence of appropriate key strokes entered on the keyboard 58, thetest is begun (100). The test processor 50 then generates a referencevoltage which is sent to the vacuum controller 18 (105) which inresponse to the signal, begins the controlled reduction of pressure inthe vacuum chamber 16. Simultaneously, the test processor 50 sends anaudio signal to the image digitizer 24 to command the image digitizer tobegin recording image data received from the video camera 22 (110). Thetest processor 50 then begins sampling an analog electrical signalproduced by the vacuum controller 18 which is proportional to thepressure in the vacuum chamber 16 (115). Concurrently, the imagedigitizer 24 is digitizing and storing digital images taken by the videocamera 22 of the wound site at a rate preferably equal to the rate atwhich the test processor 50 is sampling and digitizing pressure datafrom the vacuum controller 18, such as two frames per second (120).

The vacuum or negative pressure in the vacuum chamber 16 exerts a forceon the skin 63 surrounded by the ring 30. Since skin tissue is anelastic biomaterial, the effected skin will stretch and deflect into theinterior of the vacuum chamber 16 in a truncated spherical configurationto tend to relieve the negative pressure in the vacuum chamber. As theskin is continuously stretched by the gradually increasing vacuum, thelocator dots 66 inked on the skin 63 on either side of the wound 64 willdisplace away from the wound and away frown each other. While thepressure in the vacuum chamber 16 is continually decreased by the vacuumcontroller 18 through the communication with the vacuum source 20, thedecreasing analog voltage/pressure signal generated by the vacuumcontroller is sampled by the test processor 50 and the images of thewound area and gradually displacing dots 66 taken by the video camera 22are stored in a video format and digitized and stored in a digitalformat by the image processor 24. After a time sufficient for thepressure to have been decreased in the vacuum chamber to the point wherethe wound has ruptured, the test processor will stop the vacuum test(125).

After completion of the vacuum portion of the test, the image digitizer24 will transfer the collected image frames to the image processor 52(130). The image processor 52 will then perform standard processingtechniques on the digital images to determine the centroids of thelocator dots 66 in each image and to determine the displacement of thecentroids from the original distance between the centroids of the dotsbefore a pressure was applied to the wound area (135). Suitablealgorithms to provide such image processing functions are known in theart, and commercial software is available which has implemented thesefunctions in executable code appropriate for execution on a variety ofprocessors. Software suitable for use with the preferred imageprocessing board manufactured by Motion Analysis Corporation is alsoavailable from Motion Analysis Corporation.

Through the use of the display monitor 56 and keyboard 60 associatedwith the image processor 52, the operator may then examine thedisplacement data to identify the point of rupture of the wound, whichwill be represented in the data as a large, abrupt displacement change,and may edit the data to remove any extraneous data, such as thatcollected after the wound has ruptured or before the wound was subjectedto adequate pressure to begin the test (140). The image processor 52will then plot the displacements as a function of time on thecorresponding display monitor 56 (145) and, aided by the graphicaldisplay on the display monitor, the operator is given the option to editthe displacement data again (140). If the operator has chosen to editthe data, the edited displacement data will again be plotted as afunction of time (145). This process will continue until the operator issatisfied with the displacement data. The edited displacement data willthen be made available to the test processor 50 for correlation withedited pressure data.

The operator is given the opportunity by the test processor 50 toexamine and edit the pressure data also (150). Similar to editing thedisplacement data discussed above, the operator may choose to removeextraneous data from the pressure data, such as the pressure datacollected after the wound ruptured. The operator may also identify thepressure when the wound disrupted, which represents the burstingstrength of the wound. The test processor 50 will then plot the editedpressure data as a function of time on the display monitor 54 (155) andpermit the operator to again edit the pressure data as aided by thegraphical representation (150). Once the operator is satisfied with theedited pressure data, the test processor 50 will retrieve thedisplacement data from the image processor 52, and merge the pressureversus time data with the displacement versus time data to generatepressure (stress) versus displacement (strain) data (160). To the extentthat the pressure and displacement data points were collected atidentical points in time, they may be simply merged together; in theevent that the points are collected at slightly different points intime, they may be merged using standard interpolation techniques.

The pressure is then plotted on the display monitor 54 as a function ofdisplacement to produce a stress versus strain curve for the woundspecimen (165). By determining algorithmically or visually, through theaid of the operator, the most linear section of the stress-strain curve,the modulus of elasticity, or the slope of the curve, and the energyabsorption, or the total area under the stress-strain curve arecalculated (170). The results of the test, including the disruptionpressure, the total displacement or deformation at rupture, the modulusof elasticity, and the energy absorption are then stored in a properlyidentified file for each specimen tested (175). These stored results mayat any time be compared to the results of other individual tests or tothe results of a series of tests, and statistical data, such as meanvalues and standard deviations, may be calculated to facilitatecomparison of data and accuracy of results (180).

To illustrate results obtainable by the VCWCD method, a number oflaboratory rats weighing from 250 grams to 300 grams were prepared asdescribed above and divided into five separate groups for measuringwound healing strength each day over a period of five days. The burstingstrength results of those tests are illustrated in FIG. 5. In thefigure, the hatched columns 70 represent bursting strength inmillimeters of mercury while the standard deviation of the testsperformed each day is indicated by the length of the bracketed lines 72extending from the top of the hatched column. As is indicated in thefigure, especially in the first few days after wound healing, thestandard deviation of the VCWCD test is very small, indicating theaccuracy and repeatability of the test.

To illustrate the accuracy of the VCWCD test over the AIPPD and Instrontensiometer tests, 45 laboratory rats weighing from 250 grams to 300grams were divided into three groups and wound healing strengths studiedat 2, 7, and 14 days after wounding using each test method. Thelaboratory rats were prepared and incised as described above with theexception that only the specimens used in the VCWCD method were markedwith indicating dots. In the Instron tensiometer and AIPPD tests thespecimens were sacrificed prior to the tests, whereas in the VCWCD testthe specimens were sacrificed immediately following completion of thetests.

For the Instron tensiometer test, the abdominal skin of the laboratoryspecimen containing the wound was excised carefully from the sacrificedanimal to avoid introducing distortion in the study area. The tissue wasthen placed in the clamps of the Instron device and progressive forcewas applied until the wound disrupted. The breaking strength wascalculated based on the grams of force required to break the wound. Fortests performed using the AIPPD method, again the abdominal wounds werecarefully excised with sharp dissection to avoid distortion of the studyarea. The excised wounds were then secured on a compressing O ringoverlying a 2 cm by 1 cm hole in the top of a cylindrical pressurechamber. The air was insufflated into the chamber until the woundsdisrupted and the pressures required to break the wounds were recordedin pounds per square inch using an in-line gauge connected through theinsufflation port. Tests performed using the VCWCD method were conductedas described above.

The data generated from VCWCD and AIPPD methods were expressed as poundsper square inch while data generated from the Instron tensiometer methodwas expressed in grams per cross-sectional area. Therefore, to comparethe three methods, the data was normalized as a percent of the mean ineach data group and as expressed as the mean and standard deviation fromthe mean. The results of the three methods of wound disruption arepresented in FIG. 6 at 2, 7 and 14 days after wounding and in Table 1below at 2 days after wounding. FIG. 6 is a graph of the mean disruptionforce as a function of healing time in days. In the graph the bracketedlines 74 indicate the standard deviation at days 2, 7 and 14. The curves76, 78, 80 illustrate that there is good correlation between all threeexperimental methods and that the slopes of the curves are similar.There was no statistically significant difference between the slopes ofthe lines in any of the three methods used.

                  TABLE 1                                                         ______________________________________                                        A comparison of wound strength measurement using                              VCWCD, AIPPD and Instron tensiometer techniques at                            2 days post wounding. The data was normalized as                              a percent of mean value.                                                      OBSERVATIONS                                                                              VCWCD.sup.1                                                                              AIPPD.sup.2                                                                             INSTRON.sup.2                                ______________________________________                                        1           1.5        2.1       3.0                                          2           1.1        2.9       0.9                                          3           1.6        1.5       1.6                                          4           1.5        3.0       1.5                                          5           1.4        2.0       4.6                                          Mean ± Std Dev                                                                         1.42 ± .19                                                                            2.3 ± .63                                                                            2.48 ± 1.62                               ______________________________________                                         Std Dev = Standard Deviation                                                  .sup.1 P<.05                                                                  .sup.2 Required 8 animals for 5 observations                             

Referring to Table 1 it is seen that the VCWCD test group for day 2 hadless standard error in wound measurement than the AIPPD and Instrontensiometer methods, with a standard deviation of only 0.19 for theVCWCD method compared to 0.63 for the AIPPD and 1.62 for Instrontensiometer methods. It is further noted that in the day 2 test for theAIPPD and Instron tensiometer methods, eight animals were required toproduce the five observations recorded because the process of excisingthe wound and mounting it in the respective devices subjected the woundsto sufficient stress to cause disruption in three instances each.

A unique attribute of the VCWCD method is the ability to measure themodulus of elasticity of the wound and the energy absorption from thedisruption test. In Table 2 below the mean, standard deviation and thestandard deviation expressed as a percent of the mean value are providedfor strength, deformation and modulus of elasticity of the VCWCD testspecimens at days 2 and 7. Examination of the Table indicates thatstandard deviation is relatively small for all aspects of the VCWCD testat days 2 and 7. This further indicates that the VCWCD test producesreliable and reproducible data even for immature wounds.

While the specific embodiment of the invention described herein isadapted for the measurement of the biomechanical properties of a woundhealing in tissue, the invention has broad applicability in measuringcharacteristics of many different materials, such as silicone,polyurethane, latex, rubber, and other deformable biomechanical andmechanical materials. The invention may also provide useful informationas to the means by which certain elastic materials rupture, such as amaterial including a small perforation to determine tear strength, forexample.

                  TABLE 2                                                         ______________________________________                                        Typical VCWCD test demonstrating a comparison of                              Bursting Strength, Skin Deformation and Modulus of                            Elasticity.                                                                   Variable     n.sup.1                                                                              Mean     Std Dev % Mean.sup.2                             ______________________________________                                        Day 2                                                                         Strength (mmHg)                                                                            5      68.02    6.93    10%                                      Deformation (mm)                                                                           5       4.76     .51    11%                                      Modulus (kPa)                                                                              5      36.76    6.28    17%                                      Day 7                                                                         Strength (mmHg)                                                                            5      246.00   32.38   13%                                      Deformation (mm)                                                                           5       4.06    0.62    13%                                      Modulus (kPa)                                                                              5      214.00   29.79   14%                                      ______________________________________                                         .sup.1 Five specimens were tested.                                            .sup.2 % Mean = Indicates standard deviation as a percentage of the mean      value.                                                                   

What is claimed is:
 1. A device for measuring certain biomechanicalproperties of a healing wound in a specimen, comprising:a) means forapplying an increasing pressure over time to an area of tissuecontaining such wound, marking means on such area for facilitatingmeasurement of expansion of such area; b) pressure measurement means formeasuring the pressure as a function of time; c) camera means forobtaining a sequence of views of such area over time; d) digitizer meansfor generating a digital representation of each of such views; and e)processor means for determining a strain value from each such digitalrepresentation and for correlating each such strain value with apressure measurement corresponding to the same point in time to providea stress-strain relationship.
 2. The device of claim 1, wherein suchmarking means includes a pair of dots, one dot located on each side ofthe wound.
 3. The device of claim 1, including means for calculating themodulus of elasticity of such area from a relatively linear portion ofsuch stress-strain relationship.
 4. The device of claim 1, furtherincluding means for displaying such pressure measurements and suchstrain values and for permitting editing of such pressure measurementsand such strain values.
 5. The device of claim 1, wherein said processormeans includes a dedicated image processor.
 6. The device of claim 1,wherein said camera means is a video camera.
 7. The device of claim 1,wherein said camera means is a charge coupled device.
 8. The device ofclaim 1, further including a display monitor for the display of suchstress-strain relationship.
 9. A device for measuring certain mechanicalproperties of an elastic material, comprising:a) means for applying anincreasing pressure over time to an area of such material, such areaincluding indicia for facilitating measurement of deformation of sucharea; b) pressure measurement means for measuring the pressure as afunction of time; c) camera means for obtaining a sequence of views ofsuch area over time; d) digitizer means for generating a digitalrepresentation of each of such views; and e) processor means fordetermining a strain value from each such digital representation and forcorrelating each such strain value with a pressure measurementcorresponding to the same point in time to provide a stress-strainrelationship.
 10. The device of claim 9, wherein said camera meansincludes a video camera.
 11. The device of claim 9, wherein said camerameans includes a charge-coupled device.
 12. The device of claim 9,wherein such area is a circular area.
 13. A method of measuring themechanical properties of an elastic material, comprising the steps of:a)marking such material with indicia facilitating tracking of anyexpansion of such material during application of a force to suchmaterial; b) applying an increasing force over time to an area of suchmaterial having such indicia to cause such material to expand over time;c) measuring the force applied to such area as a function of time; d)obtaining a sequence of views of such area over time; e) generating adigital representation of each of such views; and f) determining astrain value from each of such digital representation and correlatingeach such strain value with a force measurement corresponding to thesame point in time to provide a stress-strain relationship.
 14. Themethod of claim 13, further including the step of separately plottingsuch measured force and such digital representations as a function oftime to facilitate editing such force and digital representations. 15.The method of claim 13, wherein such mechanical characteristics includemodulus of elasticity.
 16. The method of claim 13, wherein suchmechanical characteristics include energy absorption.
 17. The method ofclaim 13, further including the step of making a statistical comparisonof such mechanical characteristics with mechanical characteristicsobtained from other tests.
 18. The method of claim 13, further includingthe step of constraining such area to a circular area.